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人乳与病原体受体 DC-SIGN 的结合随胆汁盐刺激的脂肪酶(BSSL)基因多态性而变化。

Binding of human milk to pathogen receptor DC-SIGN varies with bile salt-stimulated lipase (BSSL) gene polymorphism.

机构信息

Laboratory of Experimental Virology, Department of Medical Microbiology, Academic Medical Center, University of Amsterdam, Amsterdam, The Netherlands.

出版信息

PLoS One. 2011 Feb 28;6(2):e17316. doi: 10.1371/journal.pone.0017316.

DOI:10.1371/journal.pone.0017316
PMID:21386960
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3046167/
Abstract

OBJECTIVE

Dendritic cells bind an array of antigens and DC-SIGN has been postulated to act as a receptor for mucosal pathogen transmission. Bile salt-stimulated lipase (BSSL) from human milk potently binds DC-SIGN and blocks DC-SIGN mediated trans-infection of CD4(+) T-lymphocytes with HIV-1. Objective was to study variation in DC-SIGN binding properties and the relation between DC-SIGN binding capacity of milk and BSSL gene polymorphisms.

STUDY DESIGN

ELISA and PCR were used to study DC-SIGN binding properties and BSSL exon 11 size variation for human milk derived from 269 different mothers distributed over 4 geographical regions.

RESULTS

DC-SIGN binding properties were highly variable for milks derived from different mothers and between samplings from different geographical regions. Differences in DC-SIGN binding were correlated with a genetic polymorphism in BSSL which is related to the number of 11 amino acid repeats at the C-terminus of the protein.

CONCLUSION

The observed variation in DC-SIGN binding properties among milk samples may have implications for the risk of mucosal transmission of pathogens during breastfeeding.

摘要

目的

树突状细胞结合了一系列抗原,而 DC-SIGN 被认为是黏膜病原体传播的受体。人乳中的胆盐刺激脂肪酶 (BSSL) 能够强烈结合 DC-SIGN,并阻断 DC-SIGN 介导的 HIV-1 对 CD4+T 淋巴细胞的转染。目的是研究 DC-SIGN 结合特性的变化以及母乳中 DC-SIGN 结合能力与 BSSL 基因多态性之间的关系。

研究设计

使用 ELISA 和 PCR 研究了 269 位来自 4 个地理区域的不同母亲的母乳中 DC-SIGN 结合特性和 BSSL 外显子 11 大小的变化。

结果

来自不同母亲的母乳以及不同地理区域的采样之间的 DC-SIGN 结合特性差异很大。DC-SIGN 结合的差异与 BSSL 中的遗传多态性相关,该多态性与蛋白 C 末端的 11 个氨基酸重复数有关。

结论

母乳样本中观察到的 DC-SIGN 结合特性的变化可能会影响母乳喂养期间病原体经黏膜传播的风险。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d17e/3046167/84710b70f6d1/pone.0017316.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d17e/3046167/bd2ed1d4d28e/pone.0017316.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d17e/3046167/8d7fe397ebb1/pone.0017316.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d17e/3046167/9f41cbbb6ad0/pone.0017316.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d17e/3046167/84710b70f6d1/pone.0017316.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d17e/3046167/bd2ed1d4d28e/pone.0017316.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d17e/3046167/8d7fe397ebb1/pone.0017316.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d17e/3046167/9f41cbbb6ad0/pone.0017316.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d17e/3046167/84710b70f6d1/pone.0017316.g004.jpg

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Carbohydrate-specific signaling through the DC-SIGN signalosome tailors immunity to Mycobacterium tuberculosis, HIV-1 and Helicobacter pylori.通过DC-SIGN信号体的碳水化合物特异性信号传导可调节针对结核分枝杆菌、HIV-1和幽门螺杆菌的免疫反应。
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